510(k) Report

FDA applicant

Pryor Products

Solana Beach, CA2 decisions1982–19820 recalls

FDA records 2 decisions for Pryor Products (Solana Beach, CA) in 1982: 2 510(k) clearances. Most are in product codes FOX (Stand, Infusion) and KNO (Accessories, Wheelchair). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Pryor Products’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Pryor Products since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Pryor Products by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • FOXStand, Infusion1decision
  • KNOAccessories, Wheelchair1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K820963Patient Pal I.V. WalkerPryor Products · 19821cites it

What has FDA decided for it lately?

  • K820963Patient Pal I.V. WalkerPryor Products · 1982
  • K820964Wheelchair PalPryor Products · 1982

All 2 as Pryor Products →

Other applicant names beginning “Pryor”

FDA records each applicant name separately; these may or may not be the same firm.

Pryor Medical Devices, Inc. 1